1542609-26-6

Basic information

• Product Name: C₅₃H₆₄O₃₄
• Synonyms: C₅₃H₆₄O₃₄
• CAS NO: 1542609-26-6
• Molecular Weight: 1245.07
• Mol File: 1542609-26-6.mol
• Article Data: 1

Chemical Properties

• CAS DataBase Reference: C₅₃H₆₄O₃₄(CAS DataBase Reference)
• NIST Chemistry Reference: C₅₃H₆₄O₃₄(1542609-26-6)
• EPA Substance Registry System: C₅₃H₆₄O₃₄(1542609-26-6)

Safety Data

• Hazardous Substances Data: 1542609-26-6(Hazardous Substances Data)

Upstream product

• 70223-96-0 2,2',3,3',4',6,6'-hepta-O-acetyl-β-D-cellobiosyl bromide 
• 62512-01-0 quercetin-3-O-β-D-glucopyranosyl-(1 → 4)-β-D-glucopyranoside 
• 18464-08-9 2',3',4',6'-tetra-O-acetyl-β-D-glucopyranosyl-(1->4)-2,3,6-tri-O-acetyl-β-D-glucopyranose 

Relevant articles and documents

Synthesis of quercetin glycosides and their melanogenesis stimulatory activity in B16 melanoma cells

4′-O-β-d-Glucopyranosyl-quercetin-3-O-β-d-glucopyranosyl- (1→4)-β-d-glucopyra-noside (3) was isolated from Helminthostachys zeylanica root extract as a melanogenesis acceleration compound and was synthesized using rutin as the starting material Related compounds were also synthesized to understand the structure-activity relationships in melanin biosynthesis Melanogenesis activities of the glycosides were determined by measuring intracellular melanin content in B16 melanoma cells Among the synthesized quercetin glycosides, quercetin-3-O-β-d-glucopyranoside (1), quercetin-3-O-β-d-glucopyranosyl-(1→4)-β-d-glucopyranoside (2), and 3 showed more potent intracellular melanogenesis acceleration activities than theophyline used as positive control in a dose-dependent manner with no cytotoxic effect